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Austria
In August 2011 the puzzle of my randomising symptoms finally got a name: chronic persistant lyme and neuroborreliosis. I created this blog to find and provide sharing. I guess you must be lymean to understand. ******************************** Im August 2011 bekamen all die diversen Symptome, Schmerzen, Probleme und Problemchen einen gemeinsamen Titel: chronische persistierende Lyme Neuroborreliose. Ich habe diesen Blog eröffnet, um Erfahrungen teilen zu können. Borreliose macht einsam, vielleicht muss man Borreliose haben, um das zu verstehen.

Friday, January 27, 2012

My very first blog, let's see...

Since I have found out that it is Lyme Neuroborreliosa my life has changed. I wonder how much it has changed - as nothing happened but the fact that all my temporary symptoms have a common title now. I am still the same but I am scared now and I realize that I cannot stop thinking nor talking of it, and that might be annoying to my family and friends.

For this reason I am looking for a space to talk, to release and of course to listen. Maybe there is somebody knowing how I may feel, knowing about a life with pain and fatigue. Not always like that, but often and switching from moment to moment.

Let's see... what blogging can do? (It is my very first blog, lol) 

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